Manager -2

Sun Pharma

Gurugram District

On-site

INR 1,800,000 - 2,400,000

Full time

7 days ago
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Job summary

Sun Pharma in Gurgaon is seeking a Manager-2 to drive regulatory submissions and lifecycle management for US and OAM regions. You will prepare dossiers, review CMC documents, and respond to regulatory queries to enable timely approvals.

This role requires 8–12 years of experience, an M. Pharma degree, and strong cross-functional collaboration. Join a dynamic team and contribute to global product approvals and continuous improvements.

Qualifications

  • M. Pharma degree required with 8–12 years of pharma/regulatory experience.
  • Experience with USFDA submissions and CMC modules 1–3.
  • Proven ability to prepare and review regulatory dossiers.
  • Lifecycle management, change control, and labeling approvals.
  • Strong cross-functional collaboration and project management.

Responsibilities

  • Regulatory submission of new products and variations for US/OAM regions.
  • Prepare quality dossiers and respond to queries to enable approvals.
  • Manage lifecycle, variations, annual notifications, and labeling.
  • Compile eCTD and ensure central repository of regulatory documents.

Skills

USFDA
CMC Module-1/2/3
Regulatory Submissions
Lifecycle Management
Cross-Functional Collaboration

Education

M. Pharma

Job description

Job Title:

Manager-2

Business Unit:

Regulatory Business Continuity

Job Grade:

G11A

Location:

Gurgaon

At Sun Pharma, we commit to helping you Create your own sunshine - by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community.

Are You Ready to Create Your Own Sunshine

As you enter the Sun Pharma world, you ll find yourself becoming Better every day through continuous progress. Exhibit self-drive as you Take charge and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we Thrive together and support each other s journeys.

Key Responsibilities

Regulatory submission of new products, variations, response to queries, Life cycle management for US and OAM region through preparation of quality dossiers enabling timely approvals.

Area Of Responsibility
New submissions:
  • Review prepare CMC (Chemistry, Manufacturing and Controls) dossiers for fresh submissions.
  • Review documents (Development report, scale up report, specification, stability protocol, analytical validation), etc. Before initiation of Exhibit batches for adequacy.
Approval:
  • Review prepare response to deficiency enabling approval of products filed to regulatory agency.
Lifecycle management for drug formulations:
  • Prepare and review variation, Annual notification and labelling approval for US and OAM
  • Review of change control and file variation as per country requirement
Regulatory compliance:
  • eCTD compilation
  • Ensure reposition of comprehensive product information into central repository
  • Review regulatory filing impact of variations, change controls, etc.
Competencies Required :
  • Experience of USFDA market.
  • Knowledge of CMC Module-1, 2 3.
  • CMC Dossier Preparation
  • Lifecycle Management
  • Cross-Functional Collaboration
Job Requirements
Educational Qualification -

M. Pharma

Experience -

Tenure: 8-12 Years

Your Success Matters to Us

At Sun Pharma, your success and well-being are our top priorities! We provide robust benefits and opportunities to foster personal and professional growth. Join us at Sun Pharma, where every day is an opportunity to grow, collaborate, and make a lasting impact. Let s create a brighter future together!

Disclaimer: The preceding job description has been designed to indicate the general nature and level of work performed by employee within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of incumbent(s).

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